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Scientific Reports|May 16, 2015
Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Caused by a Novel R782G Mutation in CSF1RNicola Foulds, Reuben J Pengelly, Simon R Hammans, et al.
Scientific Reports|July 27, 2016
Deleterious coding variants in multi-case families with non-syndromic cleft lip and/or palate phenotypesReuben J Pengelly, Liliana Arias, Julio Martínez, et al.
Pediatric Pulmonology|April 18, 2006
Association of improved pulmonary phenotype in Irish cystic fibrosis patients with a 3' enhancer polymorphism in alpha-1-antitrypsinJulia M Courtney, Barry J Plant, Kevin Morgan, et al.
The European Respiratory Journal|February 1, 2007
Late-onset central hypoventilation syndrome: a family genetic studyL S Doherty, J L Kiely, P C Deegan, et al.
Journal of Visualized Experiments : Jove|August 16, 2011
High-resolution endocardial and epicardial optical mapping in a sheep model of stretch-induced atrial fibrillationDavid Filgueiras-Rama, Raphael Pedro Martins, Steven R Ennis, et al.
Journal of Vascular and Interventional Radiology : JVIR|March 18, 2020
4D Flow MR Imaging to Improve Microwave Ablation Prediction Models: A Feasibility Study in an In Vivo Porcine LiverJason Chiang, Michael Loecher, Kevin Moulin, et al.
The Journal of Arthroplasty|April 26, 2023
Does Individualization of Cup Position Affect Prosthetic or Bone Impingement Following Total Hip Arthroplasty?Douglas A Dennis, Gerard H Smith, Jessica L H Phillips, et al.
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